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OUR MISSION

To Care and to Cure

The MND and Me Foundation supports people and their families living with Motor Neurone Disease (MND) in Queensland.

The Foundation delivers support programs and funds research into treatments and a cure for MND.

The MND and Me Foundation was established by Scott Sullivan, a husband and father of two children, who was diagnosed with MND in 2010 at the age of 38. Scott sadly died in April 2014.

Fast Facts

  • Each day in Australia two people die from MND and another two people are diagnosed with MND.
  • A cure for MND is yet to be found.
  • There is no effective treatment for MND and it can strike anyone at any time.
  • The average life expectancy of a person diagnosed with MND is 2.5 years.

We need your help to ensure no one faces MND alone

Donate Today

Thank you!

With your help we are continually improving the level of care to Queenslanders impacted by MND and contributing to research so one day we can live in a world without Motor Neurone Disease.

Care

Queenslanders have easier access to equipment.

Research

Over $800,000 has been given to MND Research.

Awareness

MND can strike any one at any time. There is no cure

Our MND Community

People are staying connected with their families and friends

Our work is 100% funded by community donations. Your support will make a difference at arguably the hardest time of someone’s life. Help us make sure that no one faces MND alone.

MAKE A DONATION Find out more about MND >

Meet our MND Heros

Get Involved

You can help raise awareness by sharing this page with your friends and family!